Onsite Oncology Clinical Research Coordinator

City of Hope; Irvine (CA); On-site; USD 60,000 - 90,000; Full time

Job summary

City of Hope seeks a full-time Clinical Study Coordinator to support oncology clinical trials at its Orange County facility. The role involves coordinating First in Human to Phase III and Investigator-Initiated Trials, with duties in patient recruitment, informed consent, trial coordination, data management, and regulatory compliance.

Under supervision of the Director, Clinical Research, you will ensure protocol adherence, monitor eligibility and safety, communicate with investigators and

Qualifications

• Bachelor’s degree in Science, Health or related field required.
• Minimum of 2 years research or relevant clinical experience.
• ACRP or SOCRA certification within 1 year of employment.
• IATA certification within 1 month of employment.
• GCP (Good Clinical Practice) within 1 month of employment.
• Human Subjects Protection (HSP) within 1 month of employment.
• Basic Life Support (BLS) within 1 month of employment.

Responsibilities

• Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies.
• Follow and execute clinical trial protocols and procedures.
• Coordinate participant recruitment, informed consent, and care.
• Communicate with participants, investigators, and sponsors to ensure clear understanding and compliance.
• Monitor and document participant eligibility, safety, and protocol adherence, and report adverse events promptly.
• Pursue continuous education and training opportunities, staying updated with the latest clinical research information, and maintain necessary certifications and licensure.

Skills

Regulatory knowledge

Clinical trial coordination

Patient recruitment

Informed consent

Data management

GCP compliance

Education

Bachelor’s degree in Science, Health or related field

Job description

City of Hope seeks a full-time Clinical Study Coordinator to support oncology clinical trials at its Orange County facility. The role involves coordinating First in Human to Phase III and Investigator-Initiated Trials, with duties in patient recruitment, informed consent, trial coordination, data management, and regulatory compliance.

Under supervision of the Director, Clinical Research, you will ensure protocol adherence, monitor eligibility and safety, communicate with investigators and